KR950003280A - 에폭시 아크릴레이트 - Google Patents
에폭시 아크릴레이트 Download PDFInfo
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- KR950003280A KR950003280A KR1019940015452A KR19940015452A KR950003280A KR 950003280 A KR950003280 A KR 950003280A KR 1019940015452 A KR1019940015452 A KR 1019940015452A KR 19940015452 A KR19940015452 A KR 19940015452A KR 950003280 A KR950003280 A KR 950003280A
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- hydrogen
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- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 title claims 6
- 239000004593 Epoxy Substances 0.000 claims abstract 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims abstract 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 4
- 238000009472 formulation Methods 0.000 claims abstract 4
- 239000000203 mixture Substances 0.000 claims abstract 4
- 229920002120 photoresistant polymer Polymers 0.000 claims abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- -1 cyclic anhydride Chemical class 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- 125000005647 linker group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- 239000004020 conductor Substances 0.000 abstract 1
- 229920005596 polymer binder Polymers 0.000 abstract 1
- 239000002491 polymer binding agent Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
- C09D163/10—Epoxy resins modified by unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
- C08F290/144—Polymers containing more than one epoxy group per molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/1455—Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
- C08G59/1461—Unsaturated monoacids
- C08G59/1466—Acrylic or methacrylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4284—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with other curing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4292—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- General Physics & Mathematics (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Epoxy Resins (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Materials For Photolithography (AREA)
- Parts Printed On Printed Circuit Boards (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
- Non-Metallic Protective Coatings For Printed Circuits (AREA)
- Manufacturing Of Printed Circuit Boards (AREA)
Abstract
비교적 분자량이 크고 화학적으로 가교가능한 일반식(Ⅲ) 및 (Ⅳ)의 신규 에폭시 아크릴레이트 및 카르복시기 함유 에폭시 아크릴레이트는 고도로 중합된 중합체 결합체를 부가적으로 사용하여 포토레지스트 배합물에서 사용될 수 있다. 이러한 레지스트 배합물을 특히 인쇄 배선판 및 인쇄판의 분야에서 사용되며 수성매체로부터 도포가능하고 거의 점착성이 없어 특히 도전체상에서 매우 양호한 모서리 피복율을 갖는다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 하기식(Ⅲ)의 신규 에폭시 아크릴레이트:상기식에서, Q는 수소 또는 하기식의 기이고;또는R1은 -H- 또는 -CH3이고, R2는 -H-, -CH3또는 페닐이며, T는 방향족 2관능성 화합물의 라디칼이고, M은 각각 독립적으로 수소 또는 하기식의 기이며,A는 방향족 2관능성 화합물의 라디칼이고, n은 0 내지 300의 정수이며, L은 하기식의 기이고;또는 -O-A-OM, 단, 일반식(Ⅲ)에서, 모든 라디칼 M이 동시에 수소 또는 일반식의 기인 것은 아니며 말단기 Q및 L에 존재하지 않는 라디칼 M의 10몰%이상, 바람직하기로는 20 내지 100몰%는 상기식의 기를 나타낸다.
- 제1항에 있어서, R1이 수소 또는 메틸이고 R2가 수소, 메틸 또는 페닐인 일반식(Ⅲ)의 에폭시 아크릴레이트.
- 제1항에 있어서, n이 0 내지 50의 정수이고 기호 A 및 T는 각각 독립적으로 하기식의 결합기인 일반식(Ⅲ)의 에폭시 아크릴레이트:상기식에서, R4및 R5는 각각 독립적으로 -H 또는 C1-C4알킬이고 결합기의 페닐 라디칼은 비치환 또는 브롬 치환된다.
- 승온에서, 촉매 및 중합반응 억제제의 존재하에 에틸렌성 불포화 단일카르복시산과 하기식(Ⅱ)의 후기 글리시딜화된 에폭시 수지를 반응시키는 것을 포함하는 일반식(Ⅲ)의 에폭시 아크릴레이트 제조 방법:상기식에서, E는 수소 또는 하기식의 기이고;F는 일반식 -O-A-OG 또는이고, G는 -H 또는 라디칼이며, 단, 일반식(Ⅱ)에서, 말단기 E 및 F에 존재하지 않는 라디칼 G의 10몰%이상은 일반식의 기를 나타내고, A,T 및 n은 제1항에 정의된 바와 같다.
- 하기식(Ⅳ)의 카르복시기 함유 에폭시 아크릴레이트:상기식에서, X는 수소 또는 하기식의 기이고;R3는 무수물 라디칼 제거 후의 다중카르복시산의 환형 무수물의 라디칼이며, W1은 수소 또는 하기식의 기이고;W2는 -H 또는기이며, Y는 일반식 -O-A-O-W1의 기 또는기이며, 기호 A,T,R1,R2,R3및 n은 제1항에 정의된 바와 같고, 단, 일반식(Ⅳ)에서 말단기 X 및 Y에 존재하지 않는 라디칼 W110몰%이상이 하기식의 기이고;R1및 R2는 제1항에 정의된 바와 같고 제3항은 제5항에 정의된 바와 같다.
- 승온에서, 촉매 및 중합반응 억제제의 임의 존재하에 다중카르복시산의 환형 무수물과 제1항에 정의된 바와 같은 일반식(Ⅲ)의 에폭시 아크릴레이트를 반응시키는 것을 포함하는, 제5항에 따른 일반식(Ⅳ)의 카르복시기 함유 에폭시 아크릴레이트 제조방법.
- 포토레지스트 배합물에서 아크릴레이트 성분으로서의 제1항에 정의된 바와 같은 일반식(Ⅲ)의 에폭시 아크릴레이트 용도.
- 포토레지스트 배합물에서 아크릴레이트 성분으로서의 제5항에 정의된 바와 같은 일반식(Ⅳ)의 카르복시기 함유 에폭시 아크릴레이트 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH200393 | 1993-07-02 | ||
CH93-0/2003 | 1993-07-02 |
Publications (2)
Publication Number | Publication Date |
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KR950003280A true KR950003280A (ko) | 1995-02-16 |
KR100341619B1 KR100341619B1 (ko) | 2002-11-23 |
Family
ID=4223631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019940015452A KR100341619B1 (ko) | 1993-07-02 | 1994-06-30 | 에폭시아크릴레이트 |
Country Status (9)
Country | Link |
---|---|
US (2) | US6747101B2 (ko) |
EP (2) | EP1295900B1 (ko) |
JP (2) | JP3548969B2 (ko) |
KR (1) | KR100341619B1 (ko) |
CN (1) | CN1064055C (ko) |
AT (1) | ATE233287T1 (ko) |
CA (1) | CA2127203C (ko) |
DE (2) | DE59410248D1 (ko) |
TW (1) | TW268011B (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100737723B1 (ko) * | 2001-07-27 | 2007-07-10 | 주식회사 동진쎄미켐 | 감광성 수지 조성물 |
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JP3281473B2 (ja) † | 1994-01-17 | 2002-05-13 | 日本化薬株式会社 | フレキシブルプリント配線板用レジストインキ組成物及びその硬化物 |
JP3190251B2 (ja) * | 1995-06-06 | 2001-07-23 | 太陽インキ製造株式会社 | アルカリ現像型のフレキシブルプリント配線板用光硬化性・熱硬化性樹脂組成物 |
DE10223313A1 (de) * | 2002-05-24 | 2003-12-11 | Bakelite Ag | Modifizierte Epoxyacrylate |
WO2004034147A1 (ja) * | 2002-10-08 | 2004-04-22 | Hitachi Chemical Co., Ltd. | 感光性樹脂組成物、これを用いた感光性エレメント、レジストパターンの形成方法及びプリント配線板 |
KR100529371B1 (ko) * | 2003-07-29 | 2005-11-21 | 주식회사 엘지화학 | 촉매전구체 수지조성물 및 이를 이용한 투광성 전자파차폐재 제조방법 |
DE602005022448D1 (de) * | 2004-06-28 | 2010-09-02 | Canon Kk | Ekopfs und unter verwendung dieses verfahrens erhaltener flüssigkeitsausgabekopf |
WO2006001530A2 (en) * | 2004-06-28 | 2006-01-05 | Canon Kabushiki Kaisha | Liquid discharge head manufacturing method, and liquid discharge head obtained using this method |
JP4632152B2 (ja) * | 2004-08-25 | 2011-02-16 | ナガセケムテックス株式会社 | 重合性組成物 |
US20060261267A1 (en) * | 2005-05-20 | 2006-11-23 | Agency For Science, Technology And Research | Composite MALDI matrix material and methods of using it and kits thereof in MALDI |
JP2007052120A (ja) * | 2005-08-16 | 2007-03-01 | Nec Corp | 光導波路形成用感光性樹脂組成物、光導波路及び光導波路パターンの形成方法 |
US7635552B2 (en) * | 2006-07-25 | 2009-12-22 | Endicott Interconnect Technologies, Inc. | Photoresist composition with antibacterial agent |
CN101450992B (zh) * | 2007-12-07 | 2010-12-22 | 比亚迪股份有限公司 | 一种聚合物及其制备方法和含有该聚合物的导电胶 |
GB0817795D0 (en) | 2008-09-30 | 2008-11-05 | 3M Innovative Properties Co | Fast curing oil-uptaking epozxy-based structural adhesives |
US8434229B2 (en) * | 2010-11-24 | 2013-05-07 | Canon Kabushiki Kaisha | Liquid ejection head manufacturing method |
DE102012221441A1 (de) * | 2012-11-23 | 2014-05-28 | Hilti Aktiengesellschaft | Verfahren zur Herstellung von modifizierten Epoxy(meth)acrylatharzen und ihre Verwendung |
TWI559082B (zh) | 2014-07-07 | 2016-11-21 | 財團法人工業技術研究院 | 生質材料與其形成方法與印刷電路板 |
CN104311511B (zh) * | 2014-09-17 | 2017-02-15 | 济南圣泉集团股份有限公司 | 一种低水解氯衣康酸环氧树脂的制备方法 |
CN105330820B (zh) * | 2015-11-27 | 2018-08-07 | 浙江瑞通光电材料有限公司 | 一种非对称结构改性环氧丙烯酸酯树脂及其连续法合成方法 |
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-
1994
- 1994-06-15 TW TW083105380A patent/TW268011B/zh not_active IP Right Cessation
- 1994-06-23 DE DE59410248T patent/DE59410248D1/de not_active Expired - Lifetime
- 1994-06-23 EP EP02028222A patent/EP1295900B1/de not_active Expired - Lifetime
- 1994-06-23 AT AT94810375T patent/ATE233287T1/de not_active IP Right Cessation
- 1994-06-23 DE DE59410446T patent/DE59410446D1/de not_active Expired - Fee Related
- 1994-06-23 EP EP94810375A patent/EP0632078B1/de not_active Expired - Lifetime
- 1994-06-28 US US08/268,094 patent/US6747101B2/en not_active Expired - Fee Related
- 1994-06-30 CA CA002127203A patent/CA2127203C/en not_active Expired - Fee Related
- 1994-06-30 KR KR1019940015452A patent/KR100341619B1/ko not_active IP Right Cessation
- 1994-07-01 CN CN94108125A patent/CN1064055C/zh not_active Expired - Fee Related
- 1994-07-04 JP JP17482694A patent/JP3548969B2/ja not_active Expired - Fee Related
-
2001
- 2001-08-17 US US09/932,731 patent/US6784221B2/en not_active Expired - Fee Related
-
2003
- 2003-04-30 JP JP2003126076A patent/JP2004004813A/ja active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100737723B1 (ko) * | 2001-07-27 | 2007-07-10 | 주식회사 동진쎄미켐 | 감광성 수지 조성물 |
Also Published As
Publication number | Publication date |
---|---|
US6747101B2 (en) | 2004-06-08 |
CN1103073A (zh) | 1995-05-31 |
EP1295900B1 (de) | 2006-12-06 |
EP0632078A1 (de) | 1995-01-04 |
US20040072969A1 (en) | 2004-04-15 |
EP1295900A2 (de) | 2003-03-26 |
JP3548969B2 (ja) | 2004-08-04 |
DE59410446D1 (de) | 2007-01-18 |
JP2004004813A (ja) | 2004-01-08 |
EP0632078B1 (de) | 2003-02-26 |
TW268011B (ko) | 1996-01-11 |
CA2127203A1 (en) | 1995-01-03 |
EP1295900A3 (de) | 2004-01-28 |
CN1064055C (zh) | 2001-04-04 |
KR100341619B1 (ko) | 2002-11-23 |
JPH0770281A (ja) | 1995-03-14 |
ATE233287T1 (de) | 2003-03-15 |
US6784221B2 (en) | 2004-08-31 |
DE59410248D1 (de) | 2003-04-03 |
US20020019500A1 (en) | 2002-02-14 |
CA2127203C (en) | 2006-04-25 |
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